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- source_evidence_literature type ECO_0000212 NP1021598.RAP-rjUEBLLxEke-NzfcpS-BHNox3g_j2hg1yNc5KZUCg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1021598.RAP-rjUEBLLxEke-NzfcpS-BHNox3g_j2hg1yNc5KZUCg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1021598.RAP-rjUEBLLxEke-NzfcpS-BHNox3g_j2hg1yNc5KZUCg130_provenance.
- NP1021598.RAP-rjUEBLLxEke-NzfcpS-BHNox3g_j2hg1yNc5KZUCg130_assertion description "[OI type I is associated with mutations in COL1A1 mostly due to a null allele.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1021598.RAP-rjUEBLLxEke-NzfcpS-BHNox3g_j2hg1yNc5KZUCg130_provenance.
- NP1021598.RAP-rjUEBLLxEke-NzfcpS-BHNox3g_j2hg1yNc5KZUCg130_assertion evidence source_evidence_literature NP1021598.RAP-rjUEBLLxEke-NzfcpS-BHNox3g_j2hg1yNc5KZUCg130_provenance.
- NP1021598.RAP-rjUEBLLxEke-NzfcpS-BHNox3g_j2hg1yNc5KZUCg130_assertion SIO_000772 23072183 NP1021598.RAP-rjUEBLLxEke-NzfcpS-BHNox3g_j2hg1yNc5KZUCg130_provenance.
- NP1021598.RAP-rjUEBLLxEke-NzfcpS-BHNox3g_j2hg1yNc5KZUCg130_assertion wasDerivedFrom befree-2016 NP1021598.RAP-rjUEBLLxEke-NzfcpS-BHNox3g_j2hg1yNc5KZUCg130_provenance.
- NP1021598.RAP-rjUEBLLxEke-NzfcpS-BHNox3g_j2hg1yNc5KZUCg130_assertion wasGeneratedBy ECO_0000203 NP1021598.RAP-rjUEBLLxEke-NzfcpS-BHNox3g_j2hg1yNc5KZUCg130_provenance.
- befree-2016 importedOn "2016-02-19" NP1021598.RAP-rjUEBLLxEke-NzfcpS-BHNox3g_j2hg1yNc5KZUCg130_provenance.